Association of RNA Biosignatures With Bacterial Infections in Febrile Infants Aged 60 Days or Younger

Prashant Mahajan(Wayne State University), Nathan Kuppermann(University of California, Davis), Asunción Mejías(Nationwide Children's Hospital), Nicolás M. Suárez(Nationwide Children's Hospital), Damien Chaussabel(Sidra Medical and Research Center), T. Charles Casper(University of Utah), B. Smith(Nationwide Children's Hospital), Elizabeth R. Alpern(Northwestern University), Jennifer Anders(Johns Hopkins University), Shireen M. Atabaki(Children's National), Jonathan E. Bennett(DuPont (United States)), Stephen Blumberg(Jacobi Medical Center), Bema K. Bonsu(Nationwide Children's Hospital), Dominic Borgialli(Hurley Medical Center), Anne Brayer(University of Rochester Medical Center), Lorin R. Browne(Children's Hospital of Wisconsin), Daniel M. Cohen(Nationwide Children's Hospital), Ellen F. Crain(Jacobi Medical Center), Andrea T. Cruz(Baylor College of Medicine), Peter S. Dayan(Columbia University), Rajender Gattu(University of Maryland, Baltimore), Richard A. Greenberg(Primary Children's Hospital), John D. Hoyle(Western Michigan University), David M. Jaffe(St. Louis Children's Hospital), Deborah A. Levine(Bellevue Hospital Center), Kathleen Lillis(Women & Children's Hospital of Buffalo), James G. Linakis(Brown University), Jared T. Muenzer(St. Louis Children's Hospital), Lise E. Nigrovic(Boston Children's Hospital), Elizabeth C. Powell(Northwestern University), Alexander J. Rogers(University of Michigan), Genie Roosevelt(Children's Hospital Colorado), Richard M. Ruddy(Cincinnati Children's Hospital Medical Center), Mary Saunders(Children's Hospital of Wisconsin), Michael G. Tunik(Bellevue Hospital Center), Leah Tzimenatos(University of California, Davis), elissa Vitale(University of Pittsburgh), Jurrien Dean(University of Utah), Octavio Ramilo(Nationwide Children's Hospital)
JAMA
August 23, 2016
Cited by 215Open Access
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Abstract

IMPORTANCE: Young febrile infants are at substantial risk of serious bacterial infections; however, the current culture-based diagnosis has limitations. Analysis of host expression patterns ("RNA biosignatures") in response to infections may provide an alternative diagnostic approach. OBJECTIVE: To assess whether RNA biosignatures can distinguish febrile infants aged 60 days or younger with and without serious bacterial infections. DESIGN, SETTING, AND PARTICIPANTS: Prospective observational study involving a convenience sample of febrile infants 60 days or younger evaluated for fever (temperature >38° C) in 22 emergency departments from December 2008 to December 2010 who underwent laboratory evaluations including blood cultures. A random sample of infants with and without bacterial infections was selected for RNA biosignature analysis. Afebrile healthy infants served as controls. Blood samples were collected for cultures and RNA biosignatures. Bioinformatics tools were applied to define RNA biosignatures to classify febrile infants by infection type. EXPOSURE: RNA biosignatures compared with cultures for discriminating febrile infants with and without bacterial infections and infants with bacteremia from those without bacterial infections. MAIN OUTCOMES AND MEASURES: Bacterial infection confirmed by culture. Performance of RNA biosignatures was compared with routine laboratory screening tests and Yale Observation Scale (YOS) scores. RESULTS: Of 1883 febrile infants (median age, 37 days; 55.7% boys), RNA biosignatures were measured in 279 randomly selected infants (89 with bacterial infections-including 32 with bacteremia and 15 with urinary tract infections-and 190 without bacterial infections), and 19 afebrile healthy infants. Sixty-six classifier genes were identified that distinguished infants with and without bacterial infections in the test set with 87% (95% CI, 73%-95%) sensitivity and 89% (95% CI, 81%-93%) specificity. Ten classifier genes distinguished infants with bacteremia from those without bacterial infections in the test set with 94% (95% CI, 70%-100%) sensitivity and 95% (95% CI, 88%-98%) specificity. The incremental C statistic for the RNA biosignatures over the YOS score was 0.37 (95% CI, 0.30-0.43). CONCLUSIONS AND RELEVANCE: In this preliminary study, RNA biosignatures were defined to distinguish febrile infants aged 60 days or younger with vs without bacterial infections. Further research with larger populations is needed to refine and validate the estimates of test accuracy and to assess the clinical utility of RNA biosignatures in practice.


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